This article highlights what manufacturers should prioritize and areas in which new information may still emerge, along with providing a starting point for businesses that need to familiarize themselves with the UK Conformity Assessed marking requirements.
Data integration is doing much to enhance regulatory information management. Life sciences companies are increasingly discovering useful interdependencies between data, documents and RIM processes. The next step is to put this data to work to improve efficiency.
Medical devices economic operators need to act fast to mitigate impacts of the UK withdrawal of EU in March 2019.
Uncertainty caused by Britain’s EU departure creates opportunity for its neighbor.